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1 udes pyrazinamidase and N-carbamoylsarcosine amidohydrolase.
2 ilization protein (acuC) and acetylpolyamine amidohydrolase.
3  N-acetyltransferase, and N-acetylspermidine amidohydrolase.
4 a larger class of prokaryotic and eukaryotic amidohydrolases.
5  N-terminal nucleophile structural family of amidohydrolases.
6 al mechanism of N-terminal nucleophile (Ntn)-amidohydrolases.
7 , and (iii) cleavage under the action of the amidohydrolases.
8 and can be converted back to IAA by ILR1/ILL amidohydrolases.
9 /alpha)(8)-barrel fold characteristic of the amidohydrolases.
10 vate water for hydrolysis in other class III amidohydrolases.
11 level of ceramides through N-acylsphingosine amidohydrolase 1 (ASAH1) ubiquitination, UBTD1 controls
12 ne (ARGAH1 or ARGAH2 encoding arginine [Arg] amidohydrolase-1 and -2, respectively) resulted in incre
13                                   Anandamide amidohydrolase (AAH) catalyzes the hydrolysis of arachid
14  thaliana), (1) allantoinase, (2) allantoate amidohydrolase (AAH), (3) ureidoglycine aminohydrolase,
15 in extracts of wheat seedlings possess auxin amidohydrolase activity.
16          In its crystalline form, allantoate amidohydrolase adopts a relatively open conformation.
17      Histone deacetylase and acetylpolyamine amidohydrolase also share profound functional similariti
18 ASPS, to the haloacid dehalogenase, enolase, amidohydrolase and crotonase superfamilies and to the se
19 HAEA and 15-HAEA are poor substrates for AEA amidohydrolase and do not bind to the AEA uptake carrier
20                          Two acetylpolyamine amidohydrolases, AphA and AphB, were found to be involve
21 t that neutral ceramidase (N-acylsphingosine amidohydrolase [ASAH2]) is highly expressed in tumor-inf
22 essing of other proteins such as inteins and amidohydrolases, but their mechanisms in such proteins a
23                                   Allantoate amidohydrolase catalyzes the conversion of allantoate to
24 , the activity of the cobyric acid-producing amidohydrolase CbiZ enzyme is essential for the conversi
25 istinct from the canonical pathway requiring amidohydrolase CbiZ, and heterologous expression of V. c
26 ay, of archaeal origin, depends on an AdoCbi amidohydrolase (CbiZ) enzyme to generate adenosylcobyric
27                  These results indicate that amidohydrolases contribute free IAA to the auxin pool du
28 9 is similar to that of N-carbamoylsarcosine amidohydrolase (CSHase) of Arthrobacter sp. and YcaC of
29    The enzyme penicillin acylase (penicillin amidohydrolase EC 3.5.1.11) catalyses the cleavage of th
30  N-acylase IA (or N(alpha)-acyl-l-amino acid amidohydrolase, EC 3.5.1.14).
31      omega-Amidase (omega-amidodicarboxylate amidohydrolase, EC 3.5.1.3) isolated from rat liver cyto
32 rom five functionally diverse superfamilies (amidohydrolase, enolase, glutathione transferase, haloal
33 salvaging pathway for cobinamide in which an amidohydrolase enzyme cleaves off the aminopropanol moie
34 es the function of a previously unidentified amidohydrolase enzyme that converts adenosylcobinamide t
35       The existence of an adenosylcobinamide amidohydrolase enzyme would explain the lack of an adeno
36  induces the AEA-degrading enzyme fatty acid amidohydrolase (FAAH), and inhibition of FAAH activity p
37  a membrane-bound amidohydrolase, fatty acid amidohydrolase (FAAH).
38                           An enzyme from the amidohydrolase family from Deinococcus radiodurans (Dr-O
39            Certain members of an Arabidopsis amidohydrolase family hydrolyze these conjugates to free
40 hosphate synthase, another member of the Ntn-amidohydrolase family of enzymes.
41 s how the ILR1-like indole acetic acid (IAA) amidohydrolase family of genes has functionally evolved
42 zA and AtzB proteins also belong to the same amidohydrolase family.
43  sequence signature of the Ser-Ser-Lys triad amidohydrolase family.
44 amidase is a member of the Ser-Ser-Lys triad amidohydrolase family.
45  anandamide is performed by a membrane-bound amidohydrolase, fatty acid amidohydrolase (FAAH).
46 mily; GalB is structurally distinct from the amidohydrolase fold of LigJ.
47 e nucleoside phosphorylase/hydrolase-peptide/amidohydrolase fold prior to the last universal common a
48 ogy models of a functionally uncharacterized amidohydrolase from Agrobacterium radiobacter K84 (Arad3
49 d sequence identity to TrzD, a cyanuric acid amidohydrolase, from Pseudomonas sp. strain NRRLB-12227.
50                                  We examined amidohydrolase gene expression using northern and promot
51   An ortholog for the Arabidopsis IAR3 auxin amidohydrolase gene has been isolated from wheat (TaIAR3
52 Cs) and a bacterial histone deacetylase-like amidohydrolase (HDAH) from Bordetella/Alcaligenes.
53                     We characterize here two amidohydrolases, IAR3 and ILL6, that define a second pat
54 agmatine deiminase and N-carbamoylputrescine amidohydrolase in archaea, and of S-adenosylmethionine d
55  docked each metabolite into seven different amidohydrolases in both the ground-state and the high-en
56           Acid ceramidase (N-acylsphingosine amidohydrolase) is the lysosomal enzyme required to hydr
57 terminal Gln by Nt(Q)-amidase, an N-terminal amidohydrolase, is a part of the N-end rule pathway of p
58         The enzyme is able to function as an amidohydrolase, liberating hydroxylamine from LGH with h
59 mples of enzyme superfamilies, including the amidohydrolase, metallo-beta-lactamase, and enolase supe
60  the sequence of the NTA1-encoded N-terminal amidohydrolase of the yeast Saccharomyces cerevisiae, wh
61 se (SLT), and cysteine-, histidine-dependent amidohydrolase/peptidase (CHAP) domains.
62 sis revealed a cysteine, histidine-dependent amidohydrolase/peptidase domain within PlyCA.
63 ntains a CHAP (cysteine, histidine-dependent amidohydrolase/peptidase) domain found in bacterial mure
64 d a C-terminal cysteine, histidine-dependent amidohydrolases/peptidases (CHAP) domain in its C-termin
65 sly recognized cysteine, histidine-dependent amidohydrolases/peptidases catalytic domain.
66                 AtzC is thus assigned to the amidohydrolase protein family that includes cytosine dea
67 o be homologous to metalloenzymes within the amidohydrolase protein superfamily.
68 inase and dihydroorotase, both members of an amidohydrolase protein superfamily.
69 rted efforts of a YcaO enzyme (PurCD) and an amidohydrolase (PurAH) in vivo.
70  substrate analogs are used to show that the amidohydrolase PyfA mediates intramolecular cyclization
71  residue proposed to activate water in other amidohydrolases, reduced the kcat to a much lesser exten
72 oid anandamide by an inhibitor of fatty acid amidohydrolase reduces blood pressure, cardiac contracti
73 ll fractionation studies showed that the NAE amidohydrolase, responsible for FFA production, was asso
74 nomes sequenced to date, indicating that the amidohydrolase route of ureide degradation is universal
75 extent than what has been reported for other amidohydrolases, suggesting that His-223 has a different
76                       URI is a member of the amidohydrolase superfamily (AHS), a highly divergent gro
77 e end of beta-strand 8 in all members of the amidohydrolase superfamily abstracts a proton from the m
78 hat AtzB contained the conserved mononuclear amidohydrolase superfamily active-site residues His74, H
79            These proteins are members of the amidohydrolase superfamily and are currently misannotate
80             These enzymes are members of the amidohydrolase superfamily and belong to cog0402 within
81 te hydrolase, EC 3.5.2.7) is a member of the amidohydrolase superfamily and catalyzes the conversion
82                      NagA is a member of the amidohydrolase superfamily and catalyzes the deacetylati
83 spartyl dipeptidase (IAD) is a member of the amidohydrolase superfamily and catalyzes the hydrolytic
84 possess the signature sequence motifs of the amidohydrolase superfamily and likely share the same str
85         Two uncharacterized enzymes from the amidohydrolase superfamily belonging to cog1228 were clo
86 inosa has been identified as a member of the amidohydrolase superfamily by a comprehensive amino acid
87                                          The amidohydrolase superfamily comprises a remarkable set of
88 ce alignment between HutF and members of the amidohydrolase superfamily containing mononuclear metal
89                      Dr0930, a member of the amidohydrolase superfamily in Deinococcus radiodurans, w
90                                          The amidohydrolase superfamily is a functionally diverse set
91                        Two proteins from the amidohydrolase superfamily of enzymes were cloned, expre
92 s group of enzymes is closely related to the amidohydrolase superfamily of enzymes.
93              This protein is a member of the amidohydrolase superfamily of enzymes.
94  d-aminoacylase, and dihydroorotase from the amidohydrolase superfamily of enzymes.
95  and Nocardioides spp., is reportedly in the amidohydrolase superfamily of metalloenzymes, but previo
96 is enzyme is a member of the metal-dependent amidohydrolase superfamily of the (beta/alpha)(8) TIM ba
97 ctrum characteristic of other members of the amidohydrolase superfamily replaced with cobalt.
98 etal-ion dependent esterase MGS0169 from the amidohydrolase superfamily revealed a novel active site
99                         Other members of the amidohydrolase superfamily that are not guanine deaminas
100 915 is the second enzyme from cog3618 of the amidohydrolase superfamily that does not require a dival
101            This is the first enzyme from the amidohydrolase superfamily that does not require a dival
102 e only documented example of a member in the amidohydrolase superfamily that does not require one or
103 refore the first characterized member in the amidohydrolase superfamily that represents a C-C breakin
104 the lactone is hydrolyzed by a member of the amidohydrolase superfamily to yield 2-carboxy-l-lyxonate
105 rogation of uncharacterized enzymes from the amidohydrolase superfamily using a structure-guided appr
106 otated enzymes belonging to cog3964 from the amidohydrolase superfamily were determined.
107 catalytic activities of three members of the amidohydrolase superfamily were discovered using amino a
108 beta/alpha)(8) barrel and is a member of the amidohydrolase superfamily with a single zinc in the act
109 .0 A confirms that Bh0493 is a member of the amidohydrolase superfamily with conserved residues commo
110 nd 6 that places it in a small subset of the amidohydrolase superfamily with imperfect folds.
111  been suggested to consist of members of the amidohydrolase superfamily, a large class of metallohydr
112                              A member of the amidohydrolase superfamily, BmulJ_04915 from Burkholderi
113           Uronate isomerase, a member of the amidohydrolase superfamily, catalyzes the isomerization
114 ization displays the landmark feature of the amidohydrolase superfamily, showing a metal ligand (iron
115 ructure established that LigY belongs to the amidohydrolase superfamily, unlike previously characteri
116 y further suggests that ACMSD belongs to the amidohydrolase superfamily, whose structurally character
117 he known range of reactions catalyzed by the amidohydrolase superfamily.
118 aspartyl dipeptidase into the urease-related amidohydrolase superfamily.
119 racterized ADDs, yet both are members of the amidohydrolase superfamily.
120 tion by the HPP family of enzymes within the amidohydrolase superfamily.
121 etals both argue against a connection to the amidohydrolase superfamily.
122 (8) barrel, characteristic of members of the amidohydrolase superfamily.
123 tated as nonspecific dipeptidases within the amidohydrolase superfamily.
124 r, we restricted ourselves to enzymes of the amidohydrolase superfamily.
125 e that ligates the metal in most mononuclear amidohydrolases superfamily members.
126 ene (termed Ntan1) that encode a 310-residue amidohydrolase (termed NtN-amidase) specific for N-termi
127 ryotic enzyme similar to the acetylpolyamine amidohydrolases that relied on reversible acetylation an
128 have been discovered, including the enolase, amidohydrolase, thiyl radical, crotonase, vicinal-oxygen
129 opanol group of AdoCbi using the CbiZ AdoCbi amidohydrolase to generate adenosylcobyric acid, which i
130 e methylation status of indole-3-acetic acid amidohydrolase transcripts.
131 cine aminohydrolase, and (4) ureidoglycolate amidohydrolase (UAH), catalyze the complete hydrolysis o
132           The highest activity toward NAE by amidohydrolase was observed 4 to 8 h after imbibition an
133 structure of a ternary complex of allantoate amidohydrolase with its substrate allantoate and an allo
134 nic--semialdehyde decarboxylase, a class III amidohydrolase, with a single zinc ion coordinated by Hi

 
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